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Study Title and Description

Hydroxypropylmethylcellulose and methylcellulose consumption reduce postprandial insulinemia in overweight and obese men and women.



Key Questions Addressed
1 Is this a fiber intervention study?
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Primary Publication Information
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TitleData
Title Hydroxypropylmethylcellulose and methylcellulose consumption reduce postprandial insulinemia in overweight and obese men and women.
Author Maki KC., Carson ML., Miller MP., Turowski M., Bell M., Wilder DM., Rains TM., Reeves MS.
Country Provident Clinical Research, Bloomington, IN, USA. kmaki@providentcrc.com
Year 2008
Numbers Pubmed ID: 18203894

Secondary Publication Information
There are currently no secondary publications defined for this study.


Extraction Form: Fiber Database
Arms
No arms have been defined in this extraction form.

Design Details
Question... Follow Up Answer Follow-up Answer
Year of Publication 2007
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Country of Publication United States
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What was the study design? Randomized Controlled Trial (Crossover)
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Was the study blinded? all tests were double-blinded except for one that was single-blinded
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Study diet type acute feeding study
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Level of feeding control for dietary intervention All food provided
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Sample size 49
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Is there a run-in period? No
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Is there a washout period? Yes
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Did the administered fiber dose change over the course of the study? Yes
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What is the age of the population (categorical)? Adults (20+ Years)
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Study population, mean age in years 36.6
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Study population, age range in years -
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Study Population, mean BMI, kg/m2 30.8
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Study population, BMI Range, kg/m2 -
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Baseline health status Obese/overweight
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Gender (% male) ~49
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Fiber 1-type Hydroxypropyl Methylcellulose
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Fiber 1-if combination was selected for fiber type, 1st fiber type in combination -
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Fiber 1-if combination was selected for fiber type, 2nd fiber type in combination -
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Fiber 1- dose 1 (g) 1
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Fiber 1- dose 2 (g) -
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Fiber 1-Duration of intervention 120 minutes
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Fiber 1-how was the fiber administered? Beverage
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Fiber 2-type Hydroxypropyl Methylcellulose
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Fiber 2-if combination was selected for fiber type, 1st fiber type in combination -
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Fiber 2-if combination was selected for fiber type, 2nd fiber type in combination -
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Fiber 2- dose 1 (g) 2
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Fiber 2- dose 2 (g) -
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Fiber 2-Duration of intervention 120 minutes
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Fiber 2-how was the fiber administered? Beverage
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Fiber 3-type Hydroxypropyl Methylcellulose
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Fiber 3-if combination was selected for fiber type, 1st fiber type in combination -
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Fiber 3-if combination was selected for fiber type, 2nd fiber type in combination -
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Fiber 3- dose 1 (g) 2
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Fiber 3- dose 2 (g) -
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Fiber 3-Duration of intervention 120 minutes
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Fiber 3-how was the fiber administered? Beverage
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Fiber 4-type Methylcellulose
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Fiber 4-if combination was selected for fiber type, 1st fiber type in combination -
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Fiber 4-if combination was selected for fiber type, 2nd fiber type in combination -
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Fiber 4- dose 1 (g) 4
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Fiber 4- dose 2 (g) -
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Fiber 4-Duration of intervention 120 minutes
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Fiber 4-how was the fiber administered? Beverage
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Comparator 1- what was the comparator used in the intervention? Control
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Comparator 1-dose -
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Comparator 1-duration of comparator intervention 120 minutes
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Comparator 1-how was the comparator administered to participants? Beverage
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Comparator 2- what was the comparator used in the intervention? -
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Comparator 2-dose -
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Comparator 2-duration of comparator intervention -
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Comparator 2-how was the comparator administered to participants? -
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Comparator 3- what was the comparator used in the intervention? -
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Comparator 3-dose -
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Comparator 3-duration of comparator intervention -
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Comparator 3-how was the comparator administered to participants? -
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Comparator 4- what was the comparator used in the intervention? -
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Comparator 4-dose -
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Comparator 4-duration of comparator intervention -
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Comparator 4-how was the comparator administered to participants? -
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Baseline Characteristics
No baseline characteristics have been defined for this extraction form.



Results & Comparisons

No Results found.
Adverse Events
Arm or Total Title Description Comments

Quality Dimensions
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